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Abbott

Clinical Research Associate I

Alameda, CA · On-site

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... The Opportunity The CRA will ensure quality, accuracy and integrity of clinical trial data ...

Abbott

Clinical Research Associate II

Alameda, CA · On-site

$81K - $141K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ...

Abbott

Clinical Research Associate II

Alameda, CA

$81K - $141K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ...

Abbott

Clinical Research Associate II

Alameda, CA · On-site

$81K - $141K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ...

Abbott

Clinical Research Associate I

Alameda, CA

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... The Opportunity The CRA will ensure quality, accuracy and integrity of clinical trial data ...

Abbott

Clinical Research Associate I

Alameda, CA

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... The Opportunity The CRA will ensure quality, accuracy and integrity of clinical trial data ...

Abbott

Clinical Site Lead - Dallas, TX

Dallas, TX · On-site

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Site CRA, Site Contract Associate. Train facility staff regarding protocol requirements and ...

Abbott

Principal Field Clinical Procedure Specialist

$99K - $198K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Includes headquarter and field clinical research associates (CRA). * May contact and recommend ...

Abbott

Principal Field Clinical Procedure Specialist

$99K - $198K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Includes headquarter and field clinical research associates (CRA). * May contact and recommend ...

Abbott

Principal Field Clinical Procedure Specialist

$99K - $198K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Includes headquarter and field clinical research associates (CRA). * May contact and recommend ...

All JobsCra Admired Leadership Jobs

Cra Admired Leadership information

See salary details

$12

$41

$69

How much do cra admired leadership jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for cra admired leadership in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What is CRA Admired Leadership?

CRA Admired Leadership refers to a leadership development program or philosophy designed by CRA (Charles River Associates) to cultivate exceptional leaders within organizations. The program emphasizes practical leadership skills, ethical decision-making, and fostering a positive workplace culture. It aims to help leaders inspire trust, drive performance, and effectively manage teams. CRA's Admired Leadership draws from research-based practices and real-world case studies to equip professionals with actionable strategies for leading in complex environments.

How does a CRA Admired Leadership role typically collaborate with clinical research teams to ensure study success?

In a CRA Admired Leadership role, you’ll frequently work alongside clinical research associates, study coordinators, and investigators to oversee trial progress and maintain compliance with protocols. Close collaboration is essential for addressing site challenges, streamlining communication, and ensuring data integrity. You’ll also guide teams through regulatory requirements and mentor less-experienced staff, fostering a supportive environment that contributes to high-quality study outcomes. Effective teamwork and strong leadership are key to overcoming obstacles and achieving project milestones.

What are the key skills and qualifications needed to thrive as a CRA Admired Leadership, and why are they important?

To thrive as a CRA (Clinical Research Associate), you need a solid understanding of clinical trial processes, regulatory requirements, and a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Outstanding attention to detail, strong organizational skills, and effective communication set top performers apart in this role. These skills ensure the integrity of clinical data, regulatory compliance, and successful collaboration among research teams.

What is the difference between Cra Admired Leadership vs Cra Project Coordinator?

CriteriaCra Admired LeadershipCra Project Coordinator
Required CredentialsBachelor's degree, leadership certificationsBachelor's degree, project management certifications
Work EnvironmentLeadership roles, strategic planningProject execution, team coordination
Employer & Industry UsageOrganizations seeking leadership developmentConstruction, IT, or engineering firms managing projects
Common Search & ComparisonLeadership qualities, strategic rolesProject management, coordination tasks

Cra Admired Leadership focuses on guiding teams and strategic decision-making, often requiring leadership certifications. In contrast, Cra Project Coordinator handles project execution, scheduling, and team coordination within specific projects. Both roles are vital in their industries but serve different functions—one leading, the other coordinating project activities.

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Cra Admired Leadership jobs near you
Infographic showing various Cra Admired Leadership job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Associate I

Abbott

Alameda, CA • On-site

Full-time

Medical, Retirement

Re-posted 21 days ago

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

174th of 544 rated manufacturers

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION:
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:
  • Career development with an international company where you can grow the career you dream of.
  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
  • An excellent retirement savings plan with a high employer contribution
  • Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
  • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
  • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity
The CRA will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155.
This is an on-site position in Alameda, California.
What You'll Work On
  • Perform internal clinical studies, recruit study participants, conduct informed consent discussions with study volunteers, record study data, and maintain study files.
  • Coordinate internal clinical studies from start to close-out.
  • Perform study site visits (SQV, SIV, IMV, COV), generate monitoring reports, and track resolution of action items.
  • Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures, and other applicable regulatory requirements.
  • Participate in study start up activities.
  • Assist with shipping study devices and supplies to clinical sites.
  • Perform study device accountability and reconciliation.
  • Assist senior staff in development of study-specific forms and trial-specific monitoring plans.
  • Assist senior staff in study planning, designing case report forms (CRFs), and training of study sites.
  • Maintain and audit Trial Master File (TMF) and upload to eTMF to ensure inspection readiness.
  • Perform review of clinical data listings for completeness and accuracy; and escalate issues to the Clinical Operations Manager/Study Lead as needed.
  • Proactively and effectively communicate the status of clinical studies to management.
  • Participate in the interim and final reviews of study data in preparation of regulatory submissions.
  • May interact with RA/QA in responding to audits and FDA inquiries.
  • Perform any other duties as assigned by management.

Required Qualifications
  • BS degree in life sciences preferred with minimum 0-1 year CRA/CRC/CTA experience; or combination of some education and minimum 2 yrs experience will be considered.
  • Experience in conducting medical device studies and/or in-vitro diagnostics studies preferred. Pharmaceutical background may also be considered.
  • Demonstrate excellence in teamwork, solid interpersonal and communication skills including building rapport with team members/peers, study site staff, and clinical management.
  • Working knowledge of CFR, ICH-GCP, Clinical and Regulatory Affairs
  • Flexibility in daily activities.
  • Proficient with Microsoft Suite

Preferred Qualification:
  • Previous phlebotomy experience in a clinical, laboratory, hospital, or blood donation setting.
  • Phlebotomy certification (e.g., CPT, PBT-ASCP, or equivalent) preferred.

Apply Now
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.
Divisional Information
Medical Devices
General Medical Devices:
Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.
Diabetes
We're focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology.
The base pay for this position is
$73,900.00 - $116,000.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY:
Research and Discovery
DIVISION:
ADC Diabetes Care
LOCATION:
United States > Alameda : Plaza 6 Building
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
No
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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